Heflich R H, Mittelstaedt R A, Manjanatha M G, Lyn-Cook L E, Aidoo A
Division of Genetic Toxicology, National Center for Toxicological Research, Jefferson, Arkansas 72079, USA.
Environ Mol Mutagen. 1996;28(1):5-12. doi: 10.1002/(SICI)1098-2280(1996)28:1<5::AID-EM3>3.0.CO;2-G.
Treatment of female Sprague-Dawley rats with the potent mammary gland carcinogen 7,12-dimethylbenz[a]anthracene (DMBA) results in the formation of DNA adducts with dG and dA and in the induction of 6-thioguanine-resistant (TGr) lymphocyte mutants. In this study, we have examined the types of mutations induced in TGr lymphocytes from DMBA-treated rats. DNA from 263 TGr lymphocyte clones was screened for mutations in exons 2, 3, and 8 of the hprt gene by polymerase chain reaction (PCR) amplification of the exons followed by heteroduplex analysis using denaturing gradient-gel electrophoresis. Twenty-five of the clones produced heteroduplexes in exon 2, 35 produced heteroduplexes in exon 3, and 36 produced heteroduplexes in exon 8. Direct sequence analysis of the heteroduplexes revealed 96 mutations, and at least 74 of these mutations were produced independently. Eighty-five of the total mutations were simple base pair (bp) substitutions, with A --> T and G --> T transversions being the predominant types. Seven mutations were deletions, three were complex bp substitutions, and one was an insertion. The results suggest that the types of mutations produced by DMBA in rat lymphocytes are specific to the DNA adducts produced by this compound.
用强效乳腺致癌物7,12 - 二甲基苯并[a]蒽(DMBA)处理雌性斯普拉格 - 道利大鼠,会导致DNA与鸟嘌呤(dG)和腺嘌呤(dA)形成加合物,并诱导6 - 硫鸟嘌呤抗性(TGr)淋巴细胞突变。在本研究中,我们检测了DMBA处理大鼠的TGr淋巴细胞中诱导产生的突变类型。通过对hprt基因的外显子2、3和8进行聚合酶链反应(PCR)扩增,随后使用变性梯度凝胶电泳进行异源双链分析,对263个TGr淋巴细胞克隆的DNA进行突变筛选。25个克隆在外显子2中产生了异源双链,35个在外显子3中产生了异源双链,36个在外显子8中产生了异源双链。对异源双链的直接序列分析揭示了96个突变,其中至少74个突变是独立产生的。总突变中的85个是简单碱基对(bp)替换,其中A→T和G→T颠换是主要类型。7个突变是缺失,3个是复杂的bp替换,1个是插入。结果表明,DMBA在大鼠淋巴细胞中产生的突变类型与该化合物产生的DNA加合物具有特异性。